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Gut to Brain Interaction in Autism. Role of Probiotics on Clinical, Biochemical and Neurophysiological Parameters

Gut to Brain Interaction in Autism. Role of Probiotics on Clinical, Biochemical and Neurophysiological Parameters

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02708901
Enrollment
85
Registered
2016-03-15
Start date
2015-11-30
Completion date
2018-09-30
Last updated
2019-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Autism Spectrum Disorder

Keywords

Autism Spectrum Disorder, Probiotic Vivomixx®, Gastrointestinal Symptoms, Gut-Brain Axis, Endophenotypes

Brief summary

The purpose of this study is to assess the effects of a 6-months supplementation with probiotic Vivomixx® on inflammatory and gastrointestinal (GI) biomarkers, gastrointestinal disturbances, behavioral and developmental profiles, and neurophysiological features in preschoolers with Autism Spectrum Disorders (ASD) with or without GI symptoms.

Detailed description

Autism Spectrum Disorders (ASD) are most likely multifactorial diseases in which the combination of genetic and environmental factors might have a role in the expression of the phenotype. A high incidence of gastrointestinal (GI) symptoms is reported in ASD. GI disturbances and altered gut microflora could make a child with a genetic predisposition for ASD more prone to express the ASD phenotype or increase the severity of his behavioral symptoms. The exploitation of strategies which can reduce the gut production and absorption of toxins or restore normal gut microbiota, such as probiotics may represent a non-pharmacological option in the treatment of GI disturbances in ASD. The aim of this study is to determine effects of probiotics supplementation with Vivomixx® in ASD children on specific GI symptoms, ASD core deficits, cognitive and language development, on inflammatory and gastrointestinal (GI) biomarkers and on Quantitative Electroencephalographic measures (QEEG). Vivomixx® is a probiotic mixture of 8 probiotic strains (Bifidobacterium breve, Bifidobacterium longum, Bifidobacterium infantis, Lactobacillus acidophilus, Lactobacillus plantarum, Lactobacillus paracasei, Lactobacillus bulgaricus and Streptococcus thermophilus). An additional aim of the study is to determine the environmental exposure to phthalates (chemical pollutant) in ASD children, and the possible effects of probiotic supplementation on their urinary concentrations. A group of 100 unselected preschoolers with ASD will be classified as belonging to the Gastro Intestinal (GI) group or to the Not Gastro Intestinal (NGI) group on the basis of the presence of significant GI symptoms at GI severity Index. Subjects belonging to the two groups (GI and NGI) will be blind randomized 1:1 to regular diet with probiotic Vivomixx® or with placebo for 6 months. All the participants will be assessed at the baseline, after three months and after six months from the baseline in order to evaluate the possible changes in GI symptoms, in ASD symptomatology, in other affective and behavioral comorbid symptoms, in plasmatic, urinary and fecal biomarkers related to abnormal intestinal function and in the electrophysiological patterns. The effects of treatments with probiotics on children with ASD need to be confirmed by rigorous controlled trials. Aiming to examine the impact of this treatment not only on clinical but also on neurophysiological patterns this trial sets out to provide new insights into the gut-brain connection in autism. Moreover, this study's results could add new data on the relationship between the presence of phthalates, clinical features and neurophysiological patterns in ASD.

Interventions

DIETARY_SUPPLEMENTVivomixx®

Two packets (900 billions bacteria) per os (P.O.) daily x 1 month and one packet (450 billions bacteria) P.O. daily x 5 months

DIETARY_SUPPLEMENTPlacebo

Two packets (4,4 grams of maltose and silicon dioxide x 2) P.O. daily x 1 month and one packet (4,4 grams of maltose and silicon dioxide) P.O. daily x 5 months

Sponsors

Ministry of Health, Italy
CollaboratorOTHER_GOV
Istituto di Fisiologia Clinica CNR
CollaboratorOTHER
IRCCS Fondazione Stella Maris
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Intervention model description

Randomized double blind study of dietary supplement compared to placebo

Eligibility

Sex/Gender
ALL
Age
18 Months to 72 Months
Healthy volunteers
No

Inclusion criteria

* age-range: 18-72 months * ASD diagnosis according to Diagnostic and Statistical Manual of Mental Disorders-5 (DSM-5) criteria

Exclusion criteria

* brain anomalies detected by Magnetic Resonance Imaging (MRI) * neurological syndromes or focal neurological signs * anamnesis of birth asphyxia, severe premature birth (≤ 28 gestational weeks) or perinatal injuries * epilepsy * significant sensory impairment * diagnosis of organic GI Disorder (i.e. gastroesophageal reflux, food allergies, Inflammatory Bowel Disease) * diagnosis of Coeliac Disease * special diet (i.e. gluten-free diet, casein-free diet, high-protein diet, ketogenic diet)

Design outcomes

Primary

MeasureTime frameDescription
Changes in severity level of ASD symptomatology6 monthsDelta of scores at Autism Diagnostic Observation Schedule-2

Secondary

MeasureTime frameDescription
Changes in Electroencephalogram (EEG) power6 monthsRegistration with a 128-channels digital EEG: power will be assessed within each frequency band
Changes in EEG coherence6 monthsRegistration with a 128-channels digital EEG: coherence will be assessed within each frequency band
Changes in EEG asymmetry6 monthsRegistration with a 128-channels digital EEG: asymmetry will be assessed within each frequency band
Changes in levels of serum Lipopolysaccharide6 monthsDelta of values of serum Lipopolysaccharide
Changes in levels of serum Leptin6 monthsDelta of values of serum Leptin
Changes in levels of serum Resistin6 monthsDelta of values of serum Resistin
Changes in levels of serum Tumor Necrosis Factor - alfa6 monthsDelta of values of serum Tumor Necrosis Factor - alfa
Changes in levels of serum Interleukin-6 (IL-6)6 monthsDelta of values of serum Interleukin-6 (IL-6)
Changes in levels of serum Plasminogen Activator Inhibitor-1 (PAI-1)6 monthsDelta of values of serum Plasminogen Activator Inhibitor-1 (PAI-1)
Changes in GI symptomatology3 months and 6 monthsDelta of scores at GI Severity Index
Changes in global ASD symptomatology assessed by Childhood Autism Rating Scale6 monthsDelta of scores at Childhood Autism Rating Scale
Changes in ASD symptomatology: repetitive behaviors3 months and 6 monthsDelta of scores at Repetitive Behavior Scale
Changes in ASD symptomatology: sensory profiles3 months and 6 monthsDelta of scores at Sensory Profile
Changes in global ASD symptomatology assessed by Social Communication Questionnaire3 months and 6 monthsDelta of scores at Social Communication Questionnaire
Changes in Developmental Quotient6 monthsDelta of score at Griffiths Mental Developmental Scale
Changes in Adaptive Functioning6 monthsDelta of scores at Vineland Adaptive Behavior Scale-II
Changes in Behavioral Profiles3 months and 6 monthsDelta of scores at Child Behavior Checklist 1.5-5
Changes in Parental Stress3 months and 6 monthsDelta of scores at Parenting Stress Index
Changes in levels of fecal calprotectin3 months and 6 monthsDelta of values of fecal calprotectin

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026